Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
NAFLD-which can develop into liver fibrosis, nonalcoholic steatohepatosis, cirrhosis, and hepatocellular carcinoma-is defined as an excess accumulation of fat caused by abnormal lipid metabolism and excessive reactive oxygen species (ROS) generation in hepatocytes.
|
31505325 |
2020 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Treatment of mitochondria from hepatocytes of HCC group with LUT and KAE were accompanied by loss of mitochondrial membrane potential (MMP) and mitochondrial swelling and release of cytochrome c (P < 0.001) via reactive oxygen species (ROS) generation before cytotoxicity ensued.
|
29693446 |
2019 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
These differential phenolic components presumably account for their dissimilar antioxidant properties.While <i>L. cardiaca</i> extract showed moderate biological effects, <i>M. aquatica</i> extract displayed high antioxidant activity in chemical models, and that of <i>L. dentata</i> was effective in counteracting potassium dichromate-induced ROS generation in human hepatocarcinoma cells.Moreover, <i>M. aquatica</i> extract (50 μg/mL) and its mixture (50%/50%) with <i>L. dentata</i> extract displayed an effective cytoprotective effect.
|
31382408 |
2019 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Our finding indicated an increase in mitochondrial reactive oxygen species (ROS) generation, collapse in the mitochondrial membrane potential (MMP), swelling in mitochondria, and cytochrome c release (about 1.6 fold) after exposure of mitochondria obtained from the HCC rats group with chrysin (10, 20, and 40 µM) compared to the normal rats group.
|
31708277 |
2019 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
TAK-875 decreased viability of 2D and 3D cultures of HepG2, a human hepatocarcinoma cell line, in concentration- (>50 µM) and time-dependent manners, both of which corresponded with ROS generation.
|
29429148 |
2018 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Our results showed that C1 sub-fraction of methanolic extract of <i>H. parva</i> considerably increased reactive oxygen species (ROS) generation, collapse of mitochondrial membrane potential (MMP), swelling in mitochondria and cytochrome c release only on HCC liver mitochondria.
|
29035293 |
2017 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
GL-V9 induced upregulation and mitochondrial localization of NAG-1 associates with ROS generation and cell death in hepatocellular carcinoma cells.
|
28697922 |
2017 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
The derivatives significantly reduced LAAO-induced ROS generation and cytotoxicity in human embryonic kidney (HEK 293) and hepatoma (HepG2) cell lines.
|
28803055 |
2017 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
We showed that FGF19, when overexpressed, inhibited the effect of sorafenib on ROS generation and apoptosis in HCC.
|
28069043 |
2017 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Elevated production of reactive oxygen species (ROS) and an altered redox state have frequently been observed in hepatocellular carcinoma (HCC); therefore, selective killing of HCC cells by chemotherapeutic agents that stimulate ROS generation or impair antioxidant systems may be a feasible approach in HCC chemotherapy.
|
27931237 |
2016 |
Liver carcinoma
|
0.100 |
PosttranslationalModification
|
disease |
BEFREE |
On the contrary, depletion of Hic-5 blocked constitutive and HGF-induced ROS generation and JNK phosphorylation in HCCs.
|
26416447 |
2015 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Collectively, our findings demonstrate that PKCα plays a critical role in HCC development by inducing DUOX2 expression and ROS generation, and propose a strategy to target PKCα/DUOX2 as a potential adjuvant therapy for HCC treatment.
|
26056003 |
2015 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
The main finding of the present study was that the co-localization of HBx and COXIII leads to upregulation of the mitochondrial function and ROS generation, which are associated with the oncogenesis of HBV-associated HCC.
|
25778742 |
2015 |